IP Library Granted Patent US 8,088,783
Granted Patent B2
US 8,088,783 · App. 13/082,259 · Granted Jan 3, 2012

MAPK/ERK kinase inhibitors

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Quick Facts
Patent No.
US 8,088,783
App. No.
13/082,259
Granted
Jan 3, 2012
Kind
B2
Abstract

Compounds of the substituted 1,3-dialkyl-2,4-dioxo-6-(pyrimidinylamino)-1,2,3,4-tetrahydropyrimidine-5-hydroxamic acids, show below: wherein the variables are as defined herein, and pharmaceutical compositions thereof, are provided for use as inhibitors of with MEK kinase.”

Claims (20)

1. A compound having the formula:

wherein

R 1 is pyrimidine optionally substituted with one or more substituents through available valencies selected from the group consisting of halo; nitro; cyano; hydroxy; (C 1-10 )alkoxy optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 4-12 )aryl, and hetero(C 1-10 )aryl; (C 4-12 )aryloxy; hetero(C 1-10 )aryloxy; amino; (C 1-10 )alkylamino; (C 1-10 )alkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 4-12 )aryl, and hetero(C 1-10 )aryl; halo(C 1-10 )alkyl; hydroxy(C 1-10 )alkyl; (C 3-12 )cycloalkyl(C 1-5 )alkyl; hetero(C 3-12 )cycloalkyl(C 1-10 )alkyl; aryl(C 1-10 )alkyl; hetero(C 1-10 )aryl(C 1-5 )alkyl; (C 3-12 )cycloalkyl; hetero(C 3-12 )cycloalkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, (C 1-10 )alkyl, amino, (C 1-10 )alkylamino, (C 4-12 )aryl, and hetero(C 1-10 )aryl;

R 4 is (C 1-5 )alkyl;

R 5 is (C 1-5 )alkyl; and

R 11 is selected from the group consisting of hydrogen and (C 1-10 )alkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 4-12 )aryl, and hetero(C 1-10 )aryl; (C 4-12 )aryloxy; and hetero(C 1-10 )aryloxy;

or a pharmaceutically acceptable salt thereof.

2. A compound having the formula:

wherein

R 1 is pyrimidine optionally substituted with one or more substituents through available valencies selected from the group consisting of halo; nitro; cyano; hydroxy; (C 1-10 )alkoxy optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 4-12 )aryl, and hetero(C 1-10 )aryl; (C 4-12 )aryloxy; hetero(C 1-10 )aryloxy; amino; (C 1-10 )alkylamino; (C 1-10 )alkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 4-12 )aryl, and hetero(C 1-10 )aryl; halo(C 1-10 )alkyl; hydroxy(C 1-10 )alkyl; (C 3-12 )cycloalkyl(C 1-5 )alkyl; hetero(C 3-12 )cycloalkyl(C 1-10 )alkyl; aryl(C 1-10 )alkyl; hetero(C 1-10 )aryl(C 1-5 )alkyl; (C 3-12 )cycloalkyl; hetero(C 3-12 )cycloalkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, (C 1-10 )alkyl, amino, (C 1-10 )alkylamino, (C 4-12 )aryl, and hetero(C 1-10 )aryl;

R 4 is (C 1-5 )alkyl;

R 5 is (C 1-5 )alkyl;

n is selected from the group consisting of 2, 3, 4, 5 and 6;

R 13 is selected from the group consisting of hydrogen and (C 1-5 )alkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 4-12 )aryl, and hetero(C 1-10 )aryl; and

each R 14 and R 15 is independently selected from the group consisting of hydrogen; halo; -cyano; -hydroxy, and (C 1-5 )alkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 4-12 )aryl, and hetero(C 1-10 )aryl; and hydroxy(C 1-5 )alkyl optionally substituted with one or more substituents through available valencies selected from the group consisting of hydrogen; halo, nitro, cyano, hydroxy, (C 1-10 )alkoxy, amino, (C 1-10 )alkylamino, (C 4-12 )aryl, and hetero(C 1-10 )aryl;

or a pharmaceutically acceptable salt thereof.

3. The compound according to any one of claim 1 or 2 wherein the compound is in the form of a pharmaceutically acceptable salt.

4. The compound according to any one of claim 1 or 2 , wherein the compound is present in a mixture of stereoisomers.

5. The compound according to any one of claim 1 or 2 , wherein the compound comprises a single stereoisomer.

6. A pharmaceutical composition comprising as an active ingredient a compound according to any one of claim 1 or 2 and a pharmaceutically acceptable excipient.

Continuity (3)
Continuation 12652570 · Jan 5, 2010
Continuation 11876635 · Oct 22, 2007
Related Publication 20110190261A1 · Aug 4, 2011